The invention relates to antimicrobial and/or antiviral fabric compositions comprising ascorbic acid, citric acid, sodium hypophosphite, or a mixture thereof. The ascorbic acid may be covalently attached to at least one cellulosic portion of the fabric composition. The invention also relates to methods for preparing such fabric compositions.

The invention relates to a polymeric fabric comprising an outer functional layer having hydrophobic and oleophobic characteristics made of a first compound, and a second functional layer having hydrophobic characteristics made of a second compound, wherein the first and the second compound differ from each other. Further the outer functional layer at least partly coats the second layer. Additionally, the invention relates to a method of producing a polymeric fabric and an apparatus for producing a polymeric fabric.

A liquid-crystal polyether fiber with high tensile strength has an ash content of 0.3 percent by weight or less, a degree of fusion (f) of 3 or less, and a tensile strength of 18 cN/dtex or more. The liquid-crystal polyether fiber has few residues of an anti-fusion agent and causes no fusion between filaments.

The invention relates to a method for producing an antimicrobial fabric or yarn, said method comprising the steps of immersing a fabric or yarn in an aqueous solution of a metal salt whilst simultaneously subjecting said solution to ultrasonic radiation; and removing the fabric or yarn from said solution and subsequently converting the metal salt in situ in the fabric or yarn into metal oxide nanoparticles, preferably via chemical and heat treatment. Fabrics and yarns obtained or obtainable by such method are also provided. In a further aspect the invention provides an apparatus for performing such method.

The invention relates to a method for producing an antimicrobial fabric or yarn, said method comprising the steps of immersing a fabric or yarn in an aqueous solution of a metal salt whilst simultaneously subjecting said solution to ultrasonic radiation; and removing the fabric or yarn from said solution and subsequently converting the metal salt in situ in the fabric or yarn into metal oxide nanoparticles, preferably via chemical and heat treatment. Fabrics and yarns obtained or obtainable by such method are also provided. In a further aspect the invention provides an apparatus for performing such method.

Provided are carbon fibers rich in surface functional groups, which has been recovered by thermolysis and anodization of a carbon-fiber-reinforced composite material. Also provided is a carbon-fiber-reinforced resin composition characterized by having excellent mechanical characteristics and an excellent surface appearance at a low cost as a result of using said carbon fibers.

A method for providing a bio-active layer on a surface, includes the steps of: a) ionizing a plasma gas at low temperature of 150° C. or lower, and at about atmospheric pressure, thereby creating a plasma; b) introducing a precursor into said plasma; c) exposing the surface to said plasma comprising said precursor, thereby forming a coating onto the surface. The precursors include a biological pathogen transfer inhibiting compound.

A method for providing a bio-active layer on a surface, includes the steps of: a) ionizing a plasma gas at low temperature of 150° C. or lower, and at about atmospheric pressure, thereby creating a plasma; b) introducing a precursor into said plasma; c) exposing the surface to said plasma comprising said precursor, thereby forming a coating onto the surface. The precursors include a biological pathogen transfer inhibiting compound.

A surface-treated carbon fiber having a mole ratio between a carboxyl group and an acid anhydride of 50:50 to 70:30 when measured by pyrolysis gas analysis, is manufactured by spraying a reactive gas that has been made into a plasma onto the surface of a carbon fiber and introducing a functional group into the surface of the carbon fiber.

A surface-treated carbon fiber having a mole ratio between a carboxyl group and an acid anhydride of 50:50 to 70:30 when measured by pyrolysis gas analysis, is manufactured by spraying a reactive gas that has been made into a plasma onto the surface of a carbon fiber and introducing a functional group into the surface of the carbon fiber.